Generally, the projects are processed in the order of samples (libraries) receipt. The specific number assigned by the NGS team to each project is used as a reference for further communication. #Genomic health calculator registrationServices are currently ordered per email to seqteam or to seqteam or to the members of the NGS Unit you are already in contact with.Įach service project has to be registered by filling the Project Registration Form and a relevant Sample Transfer Form – forms are sent out per email. We will find a customized solution for you. Our official portfolio is limited to the most frequently requested services. If the service or the protocol you require is not in the pricelist, please contact us. Large-scale projects require individual cost calculation. Long-read sequencing on Oxford Nanopore MinION and PromethION platformsįor consulting and assistance in planning of a sequencing experiment please contact us at seqteam or seqteam pricelist valid for MDC, Charité and BIH users is available upon request.Long-read sequencing on Pacific Biosciences Sequel II.Short-read sequencing on Illumina instruments: iSeq, MiSeq, MiniSeq, NextSeq 500, NovaSeq 6000.epigenome (ChIP-Seq, Methyl-Seq, direct RNA and DNA sequencing).whole genome, whole exome, amplicon, cfDNA), Library preparation from bulk material for diverse -Seq applications:.QC for DNA and RNA samples and sequencing libraries.Support in the experimental design of NGS projects. Consultations on NGS-related questions.The team has extensive experience implementing novel protocols, automating library preparation, and methodological development.Īvailable services and technologies include: We operate an impressive line of sequencing platforms (Illumina, PacBio, Oxford Nanopore), pipetting robots and analytical equipment.
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